Full Time
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Company

Job Details

Job Description

Roles & Responsibilities

  • Manage and maintain pharmaceutical regulatory documentation, ensuring compliance with global standards and guidelines.
  • Coordinate and track clinical trial activities, including data entry, patient enrollment support, and communication with investigators.
  • Provide administrative support for pharmacovigilance activities, such as adverse event reporting and safety data management.
  • Assist in the preparation and submission of regulatory filings to health authorities, ensuring accuracy and timeliness.

Desired Candidate Profile

  • Possesses a Bachelor's degree in Pharmacy, Pharmaceutical Sciences, or a related field.
  • Holds relevant certifications, such as a Certified Pharmacy Technician (CPhT) or equivalent.
  • Minimum 3 years of experience in pharmaceutical administration or a related role.
  • Demonstrates a strong understanding of pharmaceutical regulations and guidelines (e.g., FDA, EMA).

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